DRAP1

Information DRAP1

Description

Transcriptional repression is a general mechanism for regulating transcriptional initiation in organisms ranging from yeast to humans. Accurate initiation of transcription from eukaryotic protein-encoding genes requires the assembly of a large multiprotein complex consisting of RNA polymerase II and general transcription factors such as TFIIA, TFIIB, and TFIID. DR1 is a repressor that interacts with the TATA-binding protein (TBP) of TFIID and prevents the formation of an active transcription complex by precluding the entry of TFIIA and/or TFIIB into the preinitiation complex. The protein encoded by this gene is a corepressor of transcription that interacts with DR1 to enhance DR1-mediated repression. The interaction between this corepressor and DR1 is required for corepressor function and appears to stabilize the TBP-DR1-DNA complex. [provided by RefSeq, Jul 2008]

Full Name

DR1 associated protein 1

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
2
Peaks
80,460
Non-redundant peaks
75,294

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000175550
UniProt
Q14919
Genevisible
Q14919
RefSeq
NM_006442
Aliases
NC2-alpha
All peaks DRAP1
Download BED file
Non redundant peaks DRAP1
Download BED file
SEQUENCES DRAP1
Download FASTA file
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Datasets Table for DRAP1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
DRAP1 Hep-G2 ENCODE Homo sapiens ENCSR765MKZ 69,807
DRAP1 GM12878 GEO Homo sapiens GSE97661 10,653
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.